A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682978



Internal ID21204841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62688696..62688696hg38UCSC Ensembl
chr13:63262829..63262829hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682978
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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